EP1027037B1 - Preparation pharmaceutique comprenant du clodronate en tant que principe actif et de la cellulose microcristalline silicifiee en tant qu'excipient - Google Patents

Preparation pharmaceutique comprenant du clodronate en tant que principe actif et de la cellulose microcristalline silicifiee en tant qu'excipient Download PDF

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Publication number
EP1027037B1
EP1027037B1 EP98945336A EP98945336A EP1027037B1 EP 1027037 B1 EP1027037 B1 EP 1027037B1 EP 98945336 A EP98945336 A EP 98945336A EP 98945336 A EP98945336 A EP 98945336A EP 1027037 B1 EP1027037 B1 EP 1027037B1
Authority
EP
European Patent Office
Prior art keywords
microcrystalline cellulose
clodronate
silicified microcrystalline
tablets
pharmaceutical preparation
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP98945336A
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German (de)
English (en)
Other versions
EP1027037A1 (fr
Inventor
Veli-Matti Lehtola
Eeva-Maria Susanne Rantala
Pertti Tapani Rantala
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bayer Oy
Original Assignee
Schering Oy
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Schering Oy filed Critical Schering Oy
Priority to SI9830599T priority Critical patent/SI1027037T1/xx
Priority to DE29824938U priority patent/DE29824938U1/de
Publication of EP1027037A1 publication Critical patent/EP1027037A1/fr
Application granted granted Critical
Publication of EP1027037B1 publication Critical patent/EP1027037B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/66—Phosphorus compounds
    • A61K31/662—Phosphorus acids or esters thereof having P—C bonds, e.g. foscarnet, trichlorfon
    • A61K31/663—Compounds having two or more phosphorus acid groups or esters thereof, e.g. clodronic acid, pamidronic acid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2009—Inorganic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2022—Organic macromolecular compounds
    • A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
    • A61P3/14—Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis

Definitions

  • the object of the present invention is a pharmaceutical preparation for oral use, especially a tablet, which as its active ingredient contains a pharmacologically acceptable salt of dichloromethylene bisphosphonic acid, i.e. a clodronate, especially disodium clodronate, and which as an excipient contains silicified microcrystalline cellulose.
  • a pharmacologically acceptable salt of dichloromethylene bisphosphonic acid i.e. a clodronate, especially disodium clodronate
  • silicified microcrystalline cellulose i.e. a clodronate, especially disodium clodronate
  • Clodronate or the disodium salt of dichloromethylene bisphosphonic acid, tetrahydrate is useful for instance in the treatment and prophylaxis of disorders of the calcium metabolism, such as bone resorption, hypercalcaemia and osteoporosis. Based on its ability to form a strong complex with a Ca 2+ -ion, clodronate removes excessive calcium from the circulation, prevents calcium phosphate from dissolving from the bone and/or acts via cell-mediated mechanisms.
  • wet granulation is widely used in the pharmaceutical industry in the preparation of solid dosage forms due to the advantages it offers compared to dry granulation and direct compression. Usually the amount of excipients needed in wet granulation is less than that required for direct compression, and thus an acceptably sized tablet may be obtained. Wet granulation also provides the material to be compressed with better wetting properties and the particles comprising the resulting granulate with optimized particle size and shape. Also the amount of drug in the granules is approximately the same, and thus the content uniformity of the final preparation is generally improved.
  • silicified microcrystalline cellulose for the manufacture of clodronate preparations is that the silicon dioxide of the silicified microcrystalline cellulose may also function as a gliding agent while it also improves the properties of the microcrystalline cellulose.
  • excipients in addition to silicified microcrystalline cellulose may be used in the solid dosage forms according to the invention. These excipients are known to a person skilled in the art, and their use in the manufacture of clodronate preparations has been disclosed e.g. in EP 336 851, US 3,683,080 and US 4,234,645.
  • the preparation according to the invention may further comprise conventional gliding agents and lubricants, such as stearic acid or its salts (Mg-, Ca-), talc, starch, or a mixture of two or more gliding agents.
  • gliding agents and lubricants such as stearic acid or its salts (Mg-, Ca-), talc, starch, or a mixture of two or more gliding agents.
  • talc magnesium calcium magnesium, magnesium, magnesium, magnesium, magnesium, magnesium, magnesium, magnesium magnesium, magnesium magnesium, magnesium, magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium magnesium
  • composition comprising clodronate and silicified microcrystalline cellulose is suitable for administration not only as a tablet but also as a number of different formulations.
  • it can for example be filled in capsules, or used as granules or a powder according to the methods generally known in the art, and further coated, if desired.
  • Especially preferred are tablets and capsules.
  • Tablets were prepared with the following composition per tablet: Disodium clodronate tetrahydrate 1000 mg responding anhydrous disodium clodronate 800 mg Silicified microcrystalline cellulose 205 mg Carmellose sodium 22 mg Stearic acid 15 mg Magnesium stearate 8 mg
  • the prepared tablets may be coated with a coating solution, the composition of which per tablet may be for example the following: Methyl hydroxypropylcellulose phthalate 42.8 mg Diethyl phthalate 6.4 mg Ethanol q. s. Purified water q.s.
  • the silicified microcrystalline cellulose used (Prosolv 50, Mendell, USA) had a 2 % w/w silicon dioxide concentration.
  • the tablets were prepared essentially as described in Example 1.
  • Tablets were prepared with the following composition per tablet: Disodium clodronate tetrahydrate 1000 mg responding anhydrous disodium clodronate 800 mg Silicified microcrystalline cellulose 125 mg Carmellose sodium 22 mg Stearic acid 15 mg Magnesium stearate 8 mg
  • Tablets were prepared with the following composition per tablet: Disodium clodronate tetrahydrate 1000 mg responding anhydrous disodium clodronate 800 mg Silicified microcrystalline cellulose 132 mg Carmellose sodium 22 mg Stearic acid 15 mg Magnesium stearate 8 mg
  • Example 1 The tablets were prepared essentially as described in Example 1, using the same kind of silicified microcrystalline cellulose as in Example 1.

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Rheumatology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Inorganic Chemistry (AREA)
  • Endocrinology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Silicates, Zeolites, And Molecular Sieves (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Claims (9)

  1. Préparation pharmaceutique contenant en tant qu'ingrédient actif un sel pharmacologiquement acceptable de l'acide dichlorométhylènebisphosphonique, caractérisée en ce qu'elle se présente sous la forme d'un dosage solide pour voie orale comprenant de la cellulose microcristalline siliciée, obtenue par co-traitement de cellulose microcristalline avec une quantité d'environ 0,1 à environ 20 % de dioxyde de silicium, par rapport à la quantité de cellulose microcristalline.
  2. Préparation suivant la revendication 1, caractérisée en ce qu'elle comprend 5-25 % en poids de cellulose microcristalline siliciée.
  3. Préparation suivant la revendication 1, caractérisée en ce qu'elle comprend
    a) environ 60 à 80 % en poids de clodronate disodique anhydre ;
    b) environ 8 à 20 % en poids de cellulose microcristalline siliciée ; et
    c) environ 0,5 à 10 % en poids de lubrifiants et/ou désintégrants.
  4. Préparation suivant l'une quelconque des revendications précédentes, caractérisée en ce qu'elle se présente sous la forme d'un comprimé ou d'une gélule.
  5. Préparation suivant l'une quelconque des revendications précédentes, caractérisée en ce que le sel de l'acide dichlorométhylènebisphosphonique est le sel disodique.
  6. Procédé pour la fabrication d'une préparation pharmaceutique selon la revendication 1, caractérisé en ce qu'il comprend la mise en oeuvre d'une technique de granulation humide.
  7. Procédé pour la fabrication d'une préparation pharmaceutique selon la revendication 1, caractérisé en ce qu'il comprend la mise en oeuvre d'une technique de granulation sèche.
  8. Procédé pour la fabrication d'une préparation pharmaceutique selon la revendication 1, caractérisé en ce qu'il comprend la mise en oeuvre d'une technique de compression directe.
  9. Utilisation de cellulose microcristalline siliciée obtenue par co-traitement de cellulose microcristalline avec une quantité d'environ 0,1 à environ 20 % de dioxyde de silicium, par rapport à la quantité de cellulose microcristalline, pour la fabrication d'une préparation pharmaceutique contenant en tant qu'ingrédient actif un sel pharmacologiquement acceptable de l'acide dichlorométhylènebisphosphonique.
EP98945336A 1997-09-19 1998-09-18 Preparation pharmaceutique comprenant du clodronate en tant que principe actif et de la cellulose microcristalline silicifiee en tant qu'excipient Expired - Lifetime EP1027037B1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
SI9830599T SI1027037T1 (en) 1997-09-19 1998-09-18 Pharmaceutical preparation comprising clodronate as active ingredient and silicified microcrystalline cellulose as excipient
DE29824938U DE29824938U1 (de) 1997-09-19 1998-09-18 Pharmazeutische Zubereitung, die Clodronat als Wirkstoff und silifizierte mikrokristalline Cellulose als Exzipienten umfasst

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FI973733 1997-09-19
FI973733A FI109088B (fi) 1997-09-19 1997-09-19 Tabletti ja menetelmä sen valmistamiseksi
PCT/FI1998/000735 WO1999015155A1 (fr) 1997-09-19 1998-09-18 Preparation pharmaceutique comprenant du clodronate en tant que principe actif et de la cellulose microcristalline silicifiee en tant qu'excipient

Publications (2)

Publication Number Publication Date
EP1027037A1 EP1027037A1 (fr) 2000-08-16
EP1027037B1 true EP1027037B1 (fr) 2003-12-03

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EP98945336A Expired - Lifetime EP1027037B1 (fr) 1997-09-19 1998-09-18 Preparation pharmaceutique comprenant du clodronate en tant que principe actif et de la cellulose microcristalline silicifiee en tant qu'excipient

Country Status (31)

Country Link
EP (1) EP1027037B1 (fr)
JP (1) JP3589977B2 (fr)
KR (1) KR20010024184A (fr)
CN (1) CN1124130C (fr)
AT (1) ATE255410T1 (fr)
AU (1) AU737738B2 (fr)
BG (1) BG64886B1 (fr)
BR (1) BR9812480A (fr)
CA (1) CA2301185C (fr)
CZ (1) CZ298675B6 (fr)
DE (3) DE1027037T1 (fr)
DK (1) DK1027037T3 (fr)
EA (1) EA002331B1 (fr)
EE (1) EE04218B1 (fr)
ES (1) ES2212341T3 (fr)
FI (1) FI109088B (fr)
HK (1) HK1031325A1 (fr)
HR (1) HRP20000142B1 (fr)
HU (1) HU226118B1 (fr)
ID (1) ID24423A (fr)
IL (1) IL135130A (fr)
IS (1) IS5404A (fr)
NO (1) NO327728B1 (fr)
NZ (1) NZ503766A (fr)
PL (1) PL191166B1 (fr)
PT (1) PT1027037E (fr)
SI (1) SI1027037T1 (fr)
SK (1) SK284088B6 (fr)
TR (1) TR200000722T2 (fr)
UA (1) UA73078C2 (fr)
WO (1) WO1999015155A1 (fr)

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PT1027037E (pt) 2004-04-30
HRP20000142A2 (en) 2000-06-30
HU226118B1 (en) 2008-04-28
BR9812480A (pt) 2000-09-26
IL135130A (en) 2004-09-27
CA2301185C (fr) 2006-11-28
JP3589977B2 (ja) 2004-11-17
EA200000317A1 (ru) 2000-10-30
DK1027037T3 (da) 2004-03-15
CZ2000787A3 (cs) 2000-08-16
SK284088B6 (sk) 2004-09-08
EA002331B1 (ru) 2002-04-25
PL191166B1 (pl) 2006-03-31
DE69820287D1 (de) 2004-01-15
HK1031325A1 (en) 2001-06-15
DE1027037T1 (de) 2002-11-28
FI973733A0 (fi) 1997-09-19
EP1027037A1 (fr) 2000-08-16
NO20001417L (no) 2000-05-19
ATE255410T1 (de) 2003-12-15
NZ503766A (en) 2002-02-01
DE29824938U1 (de) 2003-07-31
WO1999015155A1 (fr) 1999-04-01
SI1027037T1 (en) 2004-04-30
CN1124130C (zh) 2003-10-15
SK3932000A3 (en) 2000-11-07
NO327728B1 (no) 2009-09-14
JP2001517616A (ja) 2001-10-09
ID24423A (id) 2000-07-20
PL339290A1 (en) 2000-12-04
AU737738B2 (en) 2001-08-30
CZ298675B6 (cs) 2007-12-19
IS5404A (is) 2000-03-14
NO20001417D0 (no) 2000-03-17
KR20010024184A (ko) 2001-03-26
UA73078C2 (uk) 2005-06-15
AU9268598A (en) 1999-04-12
EE200000096A (et) 2000-12-15
CN1270516A (zh) 2000-10-18
HUP0004383A3 (en) 2006-06-28
HUP0004383A2 (hu) 2001-08-28
BG104265A (en) 2000-11-30
CA2301185A1 (fr) 1999-04-01
FI973733A (fi) 1999-03-20
IL135130A0 (en) 2001-05-20
HRP20000142B1 (en) 2004-06-30
BG64886B1 (bg) 2006-08-31
ES2212341T3 (es) 2004-07-16
FI109088B (fi) 2002-05-31
EE04218B1 (et) 2004-02-16
DE69820287T2 (de) 2004-10-14
TR200000722T2 (tr) 2000-11-21

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